Ethylenediaminetetraacetic Acid → (5-Chloro-2-(trifluoromethoxy)phenyl)boronic acid

To a solution of the 4-chloro(trifluoromethoxy)benzene (2.0 g, 10.18 mmol) in dry tetrahydrofuran (THF, 30 ml) at −78° C., was added ethylenediaminetetraacetic acid (EDTA, 1.24 g, 10.7 mmol) followed by a 1.3 M solution of sec-butyllithium in cyclohexane (7.63 ml, 10.7 mmol) and the reaction stirred for 2 hours under nitrogen. To this reaction mixture at −78° C., was then added dropwise the preformed dimethoxyfluoroborane mixture. The reaction was stirred at −78° C. for 30 minutes, warmed to room temperature for 30 minutes, and then quenched with water (10 ml). The reaction mixture was extracted with diethyl ether (4×50 ml). The combined organic extracts were dried over MgSO4 and concentrated in vacuo. To purify, the residue was dissolved in diethyl ether (10 ml) and washed with an aqueous solution of 10% NaOH (50 ml). The aqueous layer was acidified and extracted with ethyl acetate (3×40 ml). The combined ethyl acetate extracts were dried over MgSO4 and concentrated in vacuo to afford a mixture of the title compound and its corresponding regioisomer as a white solid (0.862 g).

1. stirringThe reaction was stirred at −78° C. for 30 minutes
2. customquenched with water (10 ml)
3. extractionThe reaction mixture was extracted with diethyl ether (4×50 ml)
4. dry with materialThe combined organic extracts were dried over MgSO4
5. concentrationconcentrated in vacuo
6. customTo purify
7. dissolutionthe residue was dissolved in diethyl ether (10 ml)
8. washwashed with an aqueous solution of 10% NaOH (50 ml)
9. extractionextracted with ethyl acetate (3×40 ml)
10. dry with materialThe combined ethyl acetate extracts were dried over MgSO4
11. concentrationconcentrated in vacuo
12. customto afford

ORDレコード

ord-0d1e6e05ceb246bfac11c2f48e955d55

出典データセット

uspto-grants-2012_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US08134007B2